64Cu-SAR-bisPSMA Positron Emission Tomography: A Phase 3 Study of Participants With Biochemical Recurrence of Prostate Cancer
Conditions
Prostate Cancer, Prostate Cancer Patients With Detectable PSA Following Prostatectomy, Prostate Cancer Recurrent, Prostate Cancer Patients Who Have Brachytherapy Seed Implant, Prostate Cancer Patients Treated by Radiotherapy, CryotherapyDrugs
64Cu-SAR-bisPSMASummary
The aim for this study is to investigate the ability of 64Cu-SAR-bisPSMA PET/CT to detect recurrence of prostate cancer
Locations
3 locations Found with status Recruiting
Status
- RECRUITING
Contact Person
- Frankis Almaguel, MD
Status
- RECRUITING
Contact Person
- Luke Nordquist, MD
Status
- RECRUITING
Contact Person
- Naveen Kella, MD
Eligibility Criteria
Inclusion Criteria:
1. At least 18 years of age.
2. Signed informed consent.
3. Life expectancy ≥ 6 months as determined by the Investigator.
4. Histologically confirmed adenocarcinoma of prostate per original diagnosis and completed subsequent definitive therapy.
5. Participant potentially eligible for salvage therapy with curative intent.
6. PSA level after definitive therapy:
1. Post-radical prostatectomy: Detectable or rising PSA that is ≥ 0.2 ng/mL with a confirmatory PSA ≥ 0.2 ng/mL (per AUA recommendation) or
2. Post-radiation therapy, cryotherapy, or brachytherapy: Increase in PSA level that is elevated by ≥ 2 ng/mL above the nadir (per ASTRO-Phoenix consensus definition).
7. Participant willing to undergo biopsy of a 64Cu-SAR-bisPSMA PET-positive lesion for histological confirmation of PC, where this is safe and feasible.
8. An Eastern Cooperative Oncology performance status of 0-2.
Exclusion Criteria:
1. Participants who received investigational agent within 5 biological half-lives prior to Day 1.
2. Participants administered any high energy (>300 KeV) gamma-emitting radioisotope within 5 physical half-lives prior to Day 1.
3. Previous systemic therapy for PC (with the exception of neoadjuvant and adjuvant systemic therapy as part of the definitive therapy).
4. Ongoing treatment or treatment within 6 months of Day 1 with any systemic therapy (e.g. any investigational therapy, androgen-deprivation therapy, antiandrogen, gonadotropin-releasing hormone, luteinizing hormone-releasing hormone agonist or antagonist, chemotherapy, immunotherapy or radiotherapy) for PC.
5. Known or expected hypersensitivity to 64Cu-SAR-bisPSMA or any of its components.
6. Any serious medical condition or extenuating circumstance (including receiving the investigational product or not capable of having a PET scan) which the investigator feels may interfere with the procedures or evaluations of the study.
Study Plan
64Cu-SAR-bisPSMA 200MBq 64Cu-SAR-bisPSMA.
DRUG:
64Cu-SAR-bisPSMADescription:
All Patients will receive a single administration, a bolus injection of 200MBq 64Cu-SAR-bisPSMA
Outcome Measures
Primary Outcome Measures
Ability of 64Cu-SAR-bisPSMA PET/CT to detect recurrence of prostate cancer
Secondary Outcome Measures
To investigate the safety and tolerability of 64-CuSAR-bisPSMA
To assess the participants-level PPV of 64Cu-SAR-bisPSMA PET/CT
To assess the participant-level DR of 64Cu-SAR-bisPSMA PET/CT
To determine the efficacy of 64Cu-SAR-bisPSMA PET/CT in participants with negative or equivocal conventional imaging at baseline
To determine the effect of the composition of Reference Standard on the performance of 64Cu-SAR-bisPSMA PET/CT
To evaluate the consistency among readers and the reproducibility of the 64Cu-SAR-bisPSMA PET/CT readings
To evaluate the consistency among readers and the reproducibility of the 64Cu-SAR-bisPSMA PET/CT readings
To determine the efficacy of 64Cu-SAR-bisPSMA PET/CT in participants with negative or equivocal conventional imaging at baseline
To determine the effect of the composition of Reference Standard on the performance of 64Cu-SAR-bisPSMA PET/CT
Timeline
Last Updated
July 17, 2025Start Date
May 14, 2025Today
December 7, 2025Completion Date ( Estimated )
December 31, 2026
Sponsors of this trial
Lead Sponsor
Clarity Pharmaceuticals Ltd